Voluntary Feed Intake and Nutrient Composition in Chickens
The phenomenon of feed intake response trends to differing feed energy and protein levels is reviewed. Increased interest in this concept is attributed to problems associated with maintaining adequate feed intake in many farms. This becomes an important factor limiting productivity. Though the spectrum of factors that affect voluntary feed intake in poultry is very broad, it is important to highlight the influence of dietary factors, particularly, energy and protein densities on voluntary feed intake responses in chickens. In formulating poultry diets, the nutrient requirements of broiler chickens have frequently been expressed per unit of dietary metabolizable energy. This practice is based on the theory that birds will adjust their feed intake according to their metabolisable energy requirements. However, based on a re-evaluation of numerous research data, the application of specific nutrient-to-metabolisable energy ratios in broiler chickens becomes questionable. Many studies have shown that feed intake responses in chickens offered diets differing in feed energy and protein levels are influenced by the level of the first limiting nutrient in the feed rather than the feed energy level per se. This observation on limitations in feed intake, in effect, challenges the strongly held theory that all chickens will consume diets to meet their energy requirements and thereby achieve their genetic potential for growth. Thus, because of the important implications of these differences, both the energy and protein levels of the diet should be taken into account when formulating diets aimed at achieving optimal feed intake in growing chickens.
April 25, 2010; Accepted: April 30, 2010;
Published: July 10, 2010
Voluntary feed intake of chickens determines nutrient intake levels and thus has a great impact on efficiency of poultry production. Often, adequate feed intake is hard to maintain on many poultry operations in several farms and, thus, becomes an important factor limiting productivity. Stressors such as hot temperature, increased stocking density and reduced health status, together with genotype, influence feed intake and, thus, growth. Furthermore, dietary factors, including energy density, deficiencies or excesses of nutrients such as carbohydrates, protein and minerals can also influence feed intake in poultry. Though the spectrum of factors that affect voluntary feed intake in poultry is very broad, the purpose of this review is to highlight the influence of dietary factors, particularly energy and protein densities, on voluntary feed intake in chickens.
ENERGY REQUIREMENT OF CHICKENS
Energy by itself is not a nutrient but a property of energy yielding nutrients,
primarily carbohydrates, lipids and proteins when they are oxidized during metabolism.
Dietary energy levels have been shown to affect broiler chickens feed
intake. Plavnik et al. (1997) and Nahashon
et al. (2005) reported that as dietary energy level increases, birds
satisfy their energy needs by decreasing feed intake. Decreases in feed intake
with high energy levels in the diets of broiler chickens have also been reported
by Leeson (2000) and Veldkamp et
al. (2005). Thus, in formulating poultry diets, the nutrient requirements
of broiler chickens have frequently been expressed per unit of dietary metabolisable
energy (Gonzalez and Pesti, 1993). This practice is
based on the theory that birds will adjust their feed intake according to their
metabolisable energy requirements and was summarized by the NRC
(1984) as an absolute requirement for energy in terms of kilocalories per
kilogram of diet cannot be stated because poultry adjust their feed intake to
obtain their necessary daily requirement. However, based on a re-evaluation
of numerous research data, the NRC (1994) have revised their
previous conclusions by stating that the practice of relating nutrient concentrations
as a function of dietary metabolisable energy seems to apply more to leghorn
type chickens fed diets with a low metabolisable energy concentration while,
as a result of the over-consumption of energy on diets with a high metabolisable
energy concentration, the application of specific nutrient-to-metabolisable
energy ratios in broiler chickens and turkeys should be re-evaluated. Leeson
et al. (1996) showed that broiler chickens fed up to 25 and 49 days
of age were able to adjust their feed intake to a constant energy intake over
a range of dietary metabolisable energy levels from 11.29 to 13.80 MJ ME/kg
DM, which indicated that broiler chickens retain an innate ability to eat to
a fixed energy requirement rather than to physical capacity as was suggested
by Newcombe and Summers (1984). However, on closer observation
of the data by Leeson et al. (1996), it can be
seen that early feed intake to 25 days of age was not greatly affected by dietary
metabolisable energy concentrations over the range of 12.13 to 13.80 MJ ME/kg
DM and that it was only at the lowest metabolisable energy concentration of
11.29 MJ ME/kg DM that a significant increase in feed intake occurred. Also,
the effects of metabolisable energy concentration on feed intake were very different
between the early (0-25 days) and later (26-49 days) growth periods, with the
metabolisable energy concentration having a far greater effect on increasing
feed intake during the grower-finisher phase. This led to the overall conclusion
by these authors that broiler chickens do indeed eat to a constant metabolisable
energy intake when viewed over the entire 49-day growing period. In contrast
to the above observation, Richards (2003) observed that
modern broiler chickens selected for rapid growth do not regulate voluntary
feed intake to achieve energy balance. This altered ability of broiler chickens
to adjust feed intake due to differences in metabolisable energy density of
the diet was postulated to result from continued selection for rapid juvenile
growth rates, which may have altered hypothalamic mechanisms that regulate feed
intake in broiler chickens (Burkhart et al., 1983;
Bokkers and Koene, 2003). Other reports have also shown
no effect of dietary metabolisable energy concentration on feed intake between
two groups of broiler chickens fed ad-libitum diets containing two energy levels
of 13.38 and 15 MJ ME/kg DM.
PROTEIN AND AMINO ACID REQUIREMENTS OF CHICKENS
Proteins have been described as complex organic compounds of high molecular
weight composed of 22 different amino acids or derivatives that are linked by
peptide bonds to form a primary chain structure. As a result of steric constraints
this primary structure has been reported to form an α-helical structure
stabilized by hydrogen bonds as well as by cross-linking of individual amino
acid residues. The á-helix that describes the primary structure of the
protein has been found to be subsequently folded and arranged into more complex
secondary and tertiary structures which, with the specific number and sequences
of different amino acids, ultimately determine the biological characteristics
and functionality of the protein (Leeson and Summers, 2001;
Horton et al., 2002). Because body proteins are
in a dynamic state, with synthesis and degradation occurring continuously, an
adequate intake of dietary amino acid is required. If dietary protein or amino
acid is inadequate, there is a reduction or cessation of growth or productivity
and a withdrawal of protein from less vital body tissues to maintain the functions
of more vital tissues (NRC, 1994).
As mentioned earlier, there are 22 amino acids in body proteins and all are
physiologically essential (NRC, 1994). Nutritionally, ten
of these are indispensable because chickens are unable to synthesize them or
can not synthesize them at a rate sufficient to meet their needs. These are
methionine, lysine, threonine, leucine, valine, isoleucine, arginine, phenylalanine,
histidine and trytophan (Austic, 1995; NRC,
1994). The amino acid requirements of poultry represent the requirements
for the indispensable amino acids plus sufficient nitrogen in an appropriate
chemical form for synthesis of the dispensible amino acids. Chickens are sensitive
to the dietary balance of these amino acids (Austic, 1995).
For the diet to be used with maximum efficiency, the chicken must receive the
indispensable amino acids in the correct quantities and sufficient amino acids
to meet the dispensable amino acids for metabolic demands must be available.
The presence of adequate amounts of nonessential amino acids in the diet reduces
the necessity of synthesizing them from essential amino acids. Amino acid requirements
may be classified as those for maintenance, carcass growth, egg production and
feather growth on the basis of their respective amino acid profiles (Hurwitz
et al., 1978). In order for the bird to realize its genetic potential
and achieve the best levels of performance through maximum rates of protein
synthesis, amino acids must be provided in the necessary quantities, avoiding
both excesses and deficiencies (Sainbury, 1984). Thus,
stating dietary requirements for both protein and essential amino acids is an
appropriate way to ensure that all amino acids needed physiologically are provided.
Protein and amino acid requirements vary considerably according to the physiological
state of the bird, that is, the rate of growth or egg production. Other factors
contributing to variations in amino acid requirements of the chickens include
age, body size, sex and breed. Amino acid requirements decrease with age and
at the same time, the ideal balance of amino acids changes gradually to reflect
those of maintenance (Zubair and Leeson, 1996). For
instance, the percentage of amino acid required in the diet is the highest for
young growing animals and declines gradually to maturity, when only enough amino
acid to maintain body tissue is required (Pond et al.,
1995). The balance of amino acids needed for maintenance is not proportional
to the balance of amino acids in a birds tissues, but rather reflects
the relative rate of obligatory loss of each individual amino acid (Gous
and Morris, 1985). For this reason, the balance needed for maintenance is
considerably different from that needed for growth or egg production (Nemavhola,
2001). Dietary amino acid levels slightly below maintenance can sustain
life, but muscle mass and functions are impaired (Leeson,
1996). Matching the amino acid profile of the diet with animal requirements
is crucial for maximizing animal performance. For instance, turkey poults and
broiler chickens have high amino acid requirements to meet the needs for rapid
growth while the indigenous chickens such as the Venda breed will require less
amino acid to meet their needs because of their slow growth rate and small body
size. Because the contributions of maintenance and growth to total amino acid
requirement change with body size and the ideal amino acid profiles for maintenance
and growth are different, the composition of the ideal amino acid pattern will
change continuously during the growth period (Mack et
|| Amino acid requirements (g kg-1 feed) at different
ages of broiler chickens
|Source: NRC (1994)
Amino acid requirements at different ages of broiler chickens are shown in
Table 1, it is now well documented that male broiler chickens
have higher dietary amino acid requirements than females (Han
and Baker, 1993; Thomas et al., 1986), because
male chickens contain more protein and less fat in their weight gain (Edwards
et al., 1973; Han and Baker, 1991).
Unlike the effect of diet energy concentration, the effect of protein density
on feed intake responses in broiler chickens has not been consistent. Buyse
et al. (1992) reported that broiler chickens reared on lower protein
density of 15% crude protein in the diet increased their feed intake in an attempt
to meet their protein requirement. Contrary to these findings, a decrease in
feed intake with reduced protein density has been reported in broiler chickens
by Kemp et al. (2005) and Berhe
and Gous (2005). These authors observed that Ross 308 broiler chickens decreased
their feed intake as dietary protein content was reduced, resulting in a lower
RESPONSE TRENDS OF CHICKENS TO DIFFERING FEED ENERGY AND PROTEIN LEVELS
To be of any real value, attempts to optimize the feeding of chickens must
be capable of predicting voluntary food intake. Gous (2007)
suggested that where feed intake is seen as an input, as is most often the case,
it is not possible to optimize feeding programs successfully since the composition
of the food offered has a very important effect on voluntary food intake. As
suggested by Emmans and Fisher (1986) appetite is dependent
on the nutrient requirements of the animal and the contents of those nutrients
in the feed and hence, responses in feed intake, therefore, are not independent
of the composition of the feed and strain of the chicken as was previously believed
(Hill and Dansky, 1954).
The theory of feed intake and growth in birds proposed by Emmans
(1981, 1989) was based on the premise that birds
attempt to grow at their genetic potential, which would imply that they would
attempt to eat as much of a given feed as would be necessary to grow at that
rate. Factors that would prevent them from achieving this goal would be the
bulkiness of the feed or the inability to lose sufficient heat to the environment
in order to enable them to remain in thermal balance. This theory has been shown
to predict feed intake and hence growth and carcass composition with considerable
accuracy in birds (Ferguson and Gous, 1997; Ferguson
et al., 1997). Additionally, Cobb 500 broiler chickens (Burnham
et al., 1992) and laying hens (Gous et al.,
1987) have been shown to increase feed intake as dietary protein content
in the feed is reduced, attempting thereby, to obtain more of the limiting protein
irrespective of the feed energy level until a dietary concentration is reached
where performance is so constrained that feed intake falls. Similarly,
Mbajiorgu (2010) observed that indigenous Venda chickens increased their
feed intake with increase in feed energy level and with decrease in feed protein
content. This is contrary to the observation that broiler chickens eat to satisfy
their energy requirements (Leeson, 2000; Nahashon
et al., 2005, 2006; Veldkamp
et al., 2005), or that broiler chickens will eat less of a feed higher
in energy content than the one having a lower energy value (Palvink
et al., 1997; Nahashon et al., 2006;
Veldkamp et al., 2005). These findings together
suggest that feed intake of broiler chickens is, first and foremost, closely
linked to the feed energy level and hence birds attempt, as a priority, to adjust
their feed intakes according to the energy level of the diet.
As suggested by Mbajiorgu (2010), indigenous Venda chickens,
however, tended to behave differently in this respect. Tadelle
et al. (2000) suggested that genetic limitation influences indigenous
chicken growth responses because it affects their nutritional requirements.
Thus, one possible consequence of the intrinsic genetic limitations of indigenous
Venda chickens might be the loss of sensitivity to regulate feed intake according
to dietary energy level. The physiological explanation for the present observation
in indigenous Venda chickens is not clear and merits further investigation.
However, it has been shown that chickens will increase their feed intake in
response to marginal levels of first limiting feed nutrient, independent of
the diet energy level (Boorman, 1979) since appetite
is assumed to be dependent on the nutrient requirements of the animal and the
contents of those nutrients in the feed (Emmans and Fisher,
1986). As such, feed intake of indigenous Venda chickens may have increased
regardless of the energy value of the feed. Thus, Venda chickens ate more feed
in an attempt to meet their protein requirements, which were limiting with decreasing
dietary crude protein levels. This observation is similar to the results obtained
with broiler chickens by Burnham et al. (1992)
and with laying hens by Gous et al. (1987). These
authors observed that chickens increased their feed intake as the limiting nutrient
in the feed decreased in an attempt to obtain more of the limiting nutrient
to satisfy their requirements for that nutrient. In fact, the nutritional factors
involved in broiler chicken feed intake control mechanisms are not completely
understood. Parsons et al. (1993) pointed out
that in many experiments, where only responses to dietary energy level are involved,
such feed intake responses could be confounded with variable intake of other
nutrients such as protein and hence differences in feed intake response patterns
to limiting feed protein content observed for Ross 308 broiler chickens and
Cobb 500 chickens as indicated in Fig. 1 below. Importantly,
it is interesting to note that these differing feed intake response patterns
to limiting feed protein content were achieved regardless of the energy value
of the feed. Contrary to the above observations, Kemp et
al. (2005) and Berhe and Gous (2005) observed
that the Ross 308 strain of broiler chickens does not apparently conform to
the theory that birds attempt to consume sufficient of a feed to meet their
requirement for the first limiting nutrient in the feed as proposed by Boorman
(1979) and supported by the work of Emmans and Fisher
(1986). These authors observed that instead of increasing food intake, the
Ross 308 broiler chicken strains decreased their feed intake as dietary energy
was increased and dietary protein content reduced, resulting in a lower growth
rate than in the Cobb 500 strain whose feed intake increases as dietary protein
content is reduced (Fig. 1).
They concluded that Ross 308 broiler chickens have been selected for improved
growth and feed efficiency using high protein feeds. The authors went further
to emphasize the point that such selection results in heavier carcasses (Pym
and Solvens, 1979) and perhaps a reduced ability to fatten when faced with
feeds marginally deficient in protein. Harper and Rogers
(1965) suggested that when there is a dietary protein deficit, the free
amino acid patterns of both muscle and plasma become imbalanced and consequently
trigger the appetite regulating system to reduce feed intake. This may be the
scenario when Ross 308 broiler chickens receive feeds marginally deficient in
protein unlike the Cobb 500 and indigenous Venda chickens. Apparently, genetic
potential may influence the Ross 308 broiler chickens feeding behaviour
as it affects their nutritional requirements (Gous et
al., 1999). Ross 308 broiler chickens have a pronounced genetic advantage
for fast growth using high protein feed compared to Cobb 500 and Venda chickens
and this might explain the differences in feed intake response patterns to marginally
limiting feed protein content.
These observations on limitations in feed intake response patterns in Ross
308 broiler chickens, Cobb 500 and indigenous Venda chickens contradict the
strongly held theory that all chickens eat to satisfy their energy requirements
(Hill and Dansky, 1954; Scott et
al., 1982; Leeson et al., 1996) or that
chickens will eat less of a feed higher in energy content than the one having
a lower energy value (Nahashon et al., 2006;
Palvink et al., 1997; Veldkamp
et al., 2005). However, because of the important implications of
these differences, both the energy and protein levels of the diet should be
taken into account when formulating diets aimed at achieving optimal feed intake
in growing birds.
Apparently, the above observations by Boorman (1979),
Gous et al. (1987), Burnham et al. (1992),
Richards (2003) and Mbajiorgu (2010)
on limitations in feed intake support the revised thinking of the NRC
(1994) that some chicken strains do not adjust their feed intake to changes
in the dietary metabolisable energy density and, as a result, may be prone to
over-consume metabolisable energy in an attempt to obtain sufficiency of a limiting
nutrient when offered diets high in energy, thereby, making the long held theory
that all chickens do adjust feed intake to a constant metabolisable energy intake
to necessitate further investigation.
It is, therefore, concluded that feed intake responses in chickens offered diets differing in feed energy and protein levels are influenced by the level of the first limiting feed nutrient rather than the feed energy level per se. This observation on limitations in feed intake in effect challenges the strongly held theory that all chickens will consume diets to meet their energy requirements and thereby achieve their genetic potential for growth. However, because of the important implications of these differences, both the energy and protein levels of the diet should be taken into account when formulating diets aimed at achieving optimal feed intake in broiler chickens.
Austic, R.E., 1995. Poultry. In: Basic Animal Nutrition and Feeding, Pond, W.G., D.C. Church and K.R. Pond (Eds.). John Wiley and Sons Canada, Ltd., New York, pp: 495-515.
Aviagen, 2006. Ross Broiler Management Manual. Aviagen Ltd., Newbridge, UK.
Berhe, E.T. and R.M. Gous, 2005. Effect of dietary protein content on allometric relationships between carcass portions and body protein in Cobb and Ross broilers. Proceedings of the 24th Conference of South African Branch of WPSA, Pretoria, Jaboticabal, UNESP.
Bokkers, E.A.M. and P. Koene, 2003. Eating behavior and preprandial and postprandial correlations in male broiler and layer chickens. Br. Poult. Sci., 44: 538-544.
Direct Link |
Boorman, K.N., 1979. Regulation of Protein and Amino Acid Intake. In: Food Intake Regulation in Poultry, Boorman, K.N. and B.M. Freeman (Eds.). British Poultry Science Ltd., Edunburgh, UK., pp: 87-125.
Burkhart, C.A., J.A. Cherry, H.P. Van Krey and P.B. Siegel, 1983. Genetic selection for growth rate alters hypothalamic satiety mechanisms in chickens. Behav. Genet., 13: 295-300.
CrossRef | Direct Link |
Burnham, D., G.C. Emmans and R. Gous, 1992. Isoleucine requirements of the chicken: The effect of excess leucine and valine on the response to isoleucine. Br. Poult. Sci., 33: 71-87.
Direct Link |
Buyse, J., E. Decuypere, L. Berghman, E.R. Kuhn and F. Vandesande, 1992. The effect of dietary protein content on episodic growth hormone secretion and on heat production of male broilers chickens. Br. Poult. Sci., 33: 1101-1109.
PubMed | Direct Link |
Edwards, Jr., H.M., F. Denman, A. Abou-ashour and D. Nugara, 1973. Carcass and fatty acid composition. Poult. Sci., 52: 934-948.
Emmans, G.C. and C. Fisher, 1986. Problems in Nutritional Theory. In: Nutrient Requirements of Poultry and Nutritional Research, Fisher, C. and K.N. Boorman (Eds.). Butterworths, London, pp: 9-39.
Emmans, G.C., 1981. A Model of the Growth and Feed Intake of Ad Libitum Fed Animals, Particularly Poultry. In: Computers in Animal Production, Hillyer, G.M., C.T. Whittemore and R.G. Gunn (Eds.). British Society of Animal Production, Thames Ditton, pp: 103-110.
Emmans, G.C., 1989. The Growth of Turkeys. In: Recent Advances in Turkey Science, Nixey, C. and T.C. Grey (Eds.). Butterworths, London, pp: 135-166.
Ferguson, N.S. and R.M. Gous, 1997. The influence of heat production on voluntary food intake in growing pigs given protein deficient diets. Anim. Sci., 64: 365-378.
Ferguson, N.S., R.M. Gous and G.C. Emmans, 1997. Predicting the effects of animal variation on growth and food intake in growing pigs using stimulation modeling. Anim. Sci., 64: 513-522.
Gonzalez, M.J. and G.M. Pesti, 1993. Evaluation of the protein to energy ratio concept in broiler and turkey nutrition. Poult. Sci. J., 72: 2115-2123.
PubMed | Direct Link |
Gous, R.M. and T.R. Morris, 1985. Evaluation of a diet dilution technique for measuring the response of broiler chickens to increasing concentrations of lysine. Br. Poult. Sci., 26: 147-161.
Direct Link |
Gous, R.M., 2007. Predicting nutrient responses in poultry: Future challenges. Animal, 1: 57-65.
Direct Link |
Gous, R.M., E.T. Moran, H.R. Stilborn, G.D. Bradford and G.C. Emmans, 1999. Evaluation of the parameters needed to describe the overall growth, the chemical growth and the growth of feathers and breast muscles of broilers. Poult. Sci., 78: 812-821.
Direct Link |
Gous, R.M., M. Griessel and T.R. Morris, 1987. Effect of dietary energy concentration on the response of laying hens to amino acids. Br. Poult. Sci., 28: 427-436.
Direct Link |
Han, Y. and D.H. Baker, 1993. Effects of sex, heat stress, body weight and genetic strain on the lysine requirement of broiler chicks. Poult. Sci., 72: 701-708.
Direct Link |
Han, Y.M. and D.H. Baker, 1991. Lysine requirement of fast and slow growing broiler chicks. Poult. Sci., 70: 2108-2114.
Direct Link |
Harper, A.E. and Q.R. Rogers, 1965. Amino acid imbalance. Proc. Nutr. Soc., 24: 173-190.
Hill, F.W. and L.M. Dansky, 1954. Studies on the energy requirements of chickens. 1. The effect of dietary energy level on growth and feed consumption. Poult. Sci., 33: 112-116.
Horton, H.R., L.A. Moran, R.S. Ochs, J.D. Rawn and A. Schrimgeour, 2002. Principles of Biochemistry. 3rd Edn., Prentice Hall, Upper Saddle River, New Jersey.
Hurwitz, S., D. Sklan and I. Bartov, 1978. New formal approaches to the determination of energy and amino acid requirements of chicks. Poult. Sci., 57: 197-205.
Kemp, C., C. Fisher and M. Kenny, 2005. Genotype-nutrition interactions in broilers response to balanced protein in two commercial strains. Proceedings of the 15th European Symposium on Poultry Nutrition, Sept. 25-29, Balatonfured, Hungary, pp: 54-56.
Leeson, S. and J.D. Summers, 2001. Protein and Amino Acids. In: Scott`s Nutrition of the Chicken, Leeson, S. and J.D. Summers (Eds.). University Books, Ontario, Canada, pp: 102-175.
Leeson, S., 2000. Is feed efficiency still a useful measure of broiler performance?. Department of Animal and Poultry Science, University of Guelp, Ministry of Agriculture, Food and Rural Affairs, Canada.
Leeson, S., L. Caston and J.D. Summers, 1996. Broiler response to diet energy. Poult. Sci., 75: 529-535.
CrossRef | Direct Link |
Mack, S., D. Bercovici, G. de Groote, B. Leclercq and M. Lippens et al., 1999. Ideal amino acid profile and dietary lysine specification for broiler chickens of 20-40 days of age. Br. Poult. Sci., 40: 257-265.
Direct Link |
Mbajiorgu, C.A., 2010. Effect of dietary energy and protein ratio level on growth and productivity of indigenous Venda chickens raised in closed confinement from day-old up to 13 weeks of age. Ph.D. Thesis, Department of Animal production, Faculty of Science and Agriculture, University of Limpopo, South Africa.
NRC, 1984. Nutrient Requirements of Poultry. 8th Rev. Edn., National Academy Press, Washington, DC.
NRC., 1994. Nutrient Requirements of Poultry. 9th Edn., National Academy Press, Washington, DC., USA., ISBN-13: 9780309048927, Pages: 155.
Nahashon, S.N., N. Adefope, A. Amenyenu and D. Wright, 2005. Effect of dietary metabolisable energy and crude protein concentrations on growth performance and carcass characteristics of French guinea fowl broilers. Poult. Sci. J., 84: 337-344.
Direct Link |
Nahashon, S.N., N. Adefope, A. Amenyenu and D. Wright, 2006. Effect of varying metabolisable energy and crude protein concentrations in diets of pearl gray guinea fowl pullets 1. Growth performance. Poult. Sci. J., 85: 1847-1854.
Direct Link |
Nemavhola, Z., 2001. The effect of different diets on production performance and meat quality of the indigenous chickens. Masters of Agricultural Management (Animal Production) Dissertation, University of Limpopo, South Africa.
Newcombe, M. and J.D. Summers, 1984. Effect of previous diet on feed intake and body weight gain of broiler and Leghorn chicks. Poult. Sci. J., 63: 1237-1242.
Parsons, C.M., K.W. Koelkebeck, Y. Zhang, X. Wang and R.W. Leeper, 1993. Effect of dietary protein and added fat levels on performance of young laying hens. J. Applied Poult. Res., 2: 214-220.
Direct Link |
Plavnik, I., E. Wax, D. Sklan, I. Bartov and S. Hurwitz, 1997. The response of broiler chickens and turkey poults to dietary energy supplied either by fat or carbohydrates. Poult. Sci., 76: 1000-1005.
Direct Link |
Pond, W.G., D.C. Church and K.R. Pond, 1995. Basic Animal Nutrition and Feeding. 4th Edn., John Wiley and Sons, New York, USA., pp: 615.
Pym, R.A.E. and A.J. Solvyns, 1979. Selection for food conversion in broilers: Body composition of birds selected for increased body‐weight gain, food consumption and food conversion ratio. Br. Poult. Sci., 20: 87-97.
Richards, M.P., 2003. Genetic regulation of feed intake and energy balance in poultry. Poult. Sci., 82: 907-916.
Direct Link |
Sainbury, D., 1984. Poultry Health and Management. Granada Publishing, Great Britian.
Scott, M.L., M.C. Nesheim and R.J. Young, 1982. Nutrition of the Chicken. 3rd Edn., M.L. Scott and Associates Ithaca, New York, USA., ISBN-10: 0960272623, pp: 562.
Tadelle, D., Y. Alemu and K.J. Peters, 2000. Indigenous chickens in Ethiopia: Genetic potential and attempts at improvement. World's Poult. Sci. J., 56: 45-54.
CrossRef | Direct Link |
Thomas, O.P., A.I. Zuckerman, M. Farran and C.B. Tampling, 1986. Updated amino acid requirements of broilers. Proceedings of the Maryland Nutrition Conference, (MNC'86), College Park, MD, pp: 79-85.
Veldkamp, T., R.P. Kwakkel, P.R. Ferket and M.W.A. Verstegen, 2005. Growth responses to dietary energy and lysine at high and low ambient temperature in male Turkeys. Poult. Sci. J., 84: 273-282.
Zubair, A.K. and S. Leeson, 1996. Compensatory growth in the broiler chicken: A review. World's Poult. Sci. J., 52: 192-201.
Direct Link |